Senior Medical Writer - Join Our Innovative Team

Artech Information Systems LLC is seeking a highly skilled Medical Writer III to join our dynamic team in Cambridge. As a pivotal member of our organization, you will craft and develop high-quality scientific documents that support our clients' clinical and regulatory needs. This role demands a meticulous approach to research and an ability to translate complex scientific data into clear, concise narratives.

We are seeking a skilled and experienced Senior Medical Writer to join our dynamic team at Artech Information Systems LLC. In this role, you will be responsible for producing high-quality, scientifically accurate documents that communicate complex medical information clearly and effectively. You will collaborate with cross-functional teams to develop and deliver regulatory submissions, clinical study reports, and other essential documentation.

Join Integrated Resources, Inc. as a Medical Writer, where you will play a pivotal role in the development of high-quality medical documentation. In this dynamic position, you will collaborate with cross-functional teams to produce regulatory documents, clinical study reports, and other materials that adhere to industry standards.

Join Integrated Resources Inc. as a Medical Writer, where your expertise will contribute to the advancement of healthcare communications. In this role, you will create and edit high-quality scientific documents, ensuring clarity and compliance with regulatory standards. Collaborate with cross-functional teams to produce materials that effectively convey complex medical information.

Join our team as a Medical Writer III, where you will play a vital role in creating and maintaining high-quality medical documentation. You will collaborate with cross-functional teams to ensure that all materials meet regulatory and compliance standards. Your expertise will contribute to the advancement of medical information and communication within our organization.

Role SummaryResponsibilities: You will play a pivotal role in enhancing the company’s commercial operations and business development initiatives while supporting our objective of establishing enduring strategic partnerships with our clients.Salary: £24,500 to £26,000 per annum, commensurate with your experience.Benefits: Enjoy discretionary profit-sharing bonuses disbursed biannually, flexible working arrangements, a generous holiday allowance, private medical insurance, critical illness coverage, income protection, and full sponsorship for external training opportunities. For more details, visit our benefits page.Role Type: Available as either full-time or part-time, permanent roles.Start Date: We are looking for candidates who can start in April or May 2026; please indicate your availability in your application.Application Deadline: Submit your application by Friday 8th March 2026. We will conduct interviews shortly after this date.Location: This opportunity is based at our Global Headquarters in Cambridge.About the RoleAt Costello Medical, a globally recognized B Corp certified medical communications firm, we are experiencing rapid growth driven by our unwavering commitment to exceptional customer service and high-quality deliverables. To facilitate this expansion, we seek a motivated Business Administrator to become part of our dynamic and collaborative External Engagement team.In this capacity, you will assist in various administrative tasks related to our business development and commercial processes, including:Commercial & Negotiation SupportAssisting in the administration of commercial negotiations within the pharmaceutical and healthcare industries by preparing necessary materials, compiling historical communications, and coordinating essential documents.Utilizing Excel to create pricing documents (rate cards) by extracting data, calculating new rates, and drafting proposals.Maintaining and updating commercial data in our internal systems.Overseeing the management of the team’s shared inbox, responding to inquiries, directing requests to appropriate team members, and ensuring timely communications.Coordinating and supporting regular team meetings focused on commercial topics, including scheduling, agenda preparation, note-taking, and action item circulation.Business Development SupportAssisting in business development initiatives and campaigns for our client-facing teams.Conducting research on client pipelines and facilitating outreach efforts to enhance engagement.

As a Principal Medical Writer at Sobi, you will leverage your expertise in communication to spearhead a strategy-oriented approach in crafting pivotal clinical and regulatory documents. Your role will be crucial in ensuring clarity, credibility, and consistency of clinical information across submission packages and clinical programs, thereby facilitating regulatory assessment and achieving product labels that meet commercial needs.Key Responsibilities:Lead an effective strategy for authoring clinical components of regulatory submissions, ensuring that the scientific content is clear, concise, complete, credible, and compelling, aligned with regulatory document objectives.Take the lead in preparing essential clinical and regulatory documents, including those that support major regulatory submissions and responses to regulatory agencies/health authorities.Provide leadership and project coordination to cross-functional authoring teams, ensuring timely delivery, high quality, and compliance with regulatory standards for clinical documents.Collaborate with senior project staff to develop a storyboard for submissions and plan document development to optimally support the proposed prescribing information.Serve as a Product Medical Writer, offering strategic medical writing expertise and support across multiple projects within a clinical development program.Ensure that all documents meet high technical quality standards in accordance with in-house technical requirements.Mentor and develop less experienced Medical Writers.Oversee and coordinate the contributions of all Medical Writers involved in documents under your purview, including in-house consultants and Medical Writers at Contract Research Organizations (CROs).

We are seeking a skilled and detail-oriented Medical Coder to join our dedicated team at Integrated Resources Inc. As a Medical Coder, you will play a crucial role in ensuring the accurate coding of medical records, which is essential for billing and insurance processes.Your responsibilities will include reviewing clinical documentation, assigning appropriate codes using ICD, CPT, and HCPCS coding systems, and collaborating with healthcare professionals to resolve discrepancies. We are looking for a candidate who is meticulous, has a strong understanding of medical terminology, and is committed to maintaining the highest coding standards.

We are seeking a highly skilled and motivated SOP Writer III to join our dynamic team in Cambridge. The ideal candidate will play a crucial role in developing and refining standard operating procedures (SOPs) that ensure operational excellence across the organization. This is an exciting opportunity to contribute to the success of our projects through meticulous documentation and process improvement.

We are seeking a highly skilled SOP Writer III to join our dynamic team. In this role, you will be responsible for developing and refining Standard Operating Procedures (SOPs) that adhere to industry regulations and ensure operational excellence. The ideal candidate will possess a keen eye for detail and a strong understanding of technical writing principles.

The Opportunity: Join Relay Therapeutics as a Senior Medical Director, where you will be pivotal in propelling our clinical pipeline from IND to proof of concept and ultimately to registration. In this role, you will partner with senior medical staff to shape clinical strategies, design clinical trials, and ensure successful execution. Collaborating across various functions including clinical project management, regulatory affairs, clinical operations, biostatistics, data management, and medical writing, you will significantly contribute as Relay Therapeutics continues to advance product candidates into clinical settings. You will provide clinical leadership to R&D teams and closely collaborate with Development leadership. We are open to remote employees

Your Contribution at Lila Lila Sciences is in search of a skilled and knowledgeable Technical Science Writer / Content Creator to play a pivotal role in articulating our scientific endeavors. This position resembles that of a managing editor, where you will convert intricate scientific concepts into precise and comprehensible content, while also mentoring a select group of contract writers to maintain exceptional storytelling quality. This role is crucial as impactful science can only transform the world when it is both understood and trusted. Your contributions will assist: Customers in grasping what Lila enables, its functionality, and its reliability. Partners in identifying opportunities for collaboration and understanding effective integration. Government and public-sector partners in evaluating relevance, safety, and societal benefits. Investors in comprehending the technical advantages, platform strategy, and long-term vision. Future employees in recognizing our ambitions, rigorous standards, and the challenges they will tackle. Your Responsibilities Draft and refine high-quality articles, explainers, technical summaries, case studies, and multimedia scripts that convey complex scientific themes with precision and narrative strength. Produce content that links what we are developing to its significance, emphasizing scientific integrity, measurable outcomes, and responsible communication. Targeted Storytelling Customize messaging and formats to meet the diverse needs of stakeholders: Customers: practical results, workflows, reliability, and real-world constraints. Partners: collaborative roadmaps, innovation narratives, and integration stories. Government entities: public benefits, validation, safety, and responsible use. Investors: distinctiveness, defensibility, and platform direction. Candidates: our mission, culture of rigor, and the problems they will address. Develop “layered” content assets, allowing a core story to be adapted across various formats (e.g., social media posts, blogs, technical briefs, presentations). Editorial Leadership Delegate tasks to contract writers, establish clear guidelines, and provide constructive feedback to ensure quality, coherence, and a consistent voice.

Are you interested in exploring future career opportunities at Lila Sciences? Even if you don't see a position that aligns perfectly with your skills and background right now, we invite you to join our talent community. By signing up, you'll be among the first to know about exciting roles that may open up in the future.

About MealSuiteAt MealSuite, we are at the forefront of revolutionizing foodservice technology tailored for healthcare and senior living sectors. Our mission is to empower care teams to provide outstanding dining experiences with minimal effort. As a rapidly expanding team, we tackle significant challenges that have a direct influence on the quality of patient and resident care.About the RoleWe are looking for a Senior Software Engineer to join us in designing, building, and maintaining the foundational systems that drive the MealSuite platform. This pivotal role will be integral in executing our product roadmap initiatives, enhancing system performance, and maintaining high standards of code quality across our Ruby on Rails applications. You will work closely with Product, Design, and Engineering teams to create scalable solutions while mentoring fellow developers and helping shape our technical architecture.What You’ll Do• Design, develop, and maintain scalable Ruby on Rails applications and services• Take ownership of features from design through deployment, testing, and support• Troubleshoot complex issues and enhance application performance, database queries, and system reliability• Perform code reviews and advocate for engineering best practices, security standards, and code quality• Contribute to architectural decisions and advancements in our technology stack• Collaborate with Product, Design, and QA to align business needs with technical solutions• Engage in Agile ceremonies and provide clear updates on progress and obstacles• Mentor junior developers and promote knowledge sharing within the engineering teamWhat You Bring• Extensive experience in building production applications using Ruby on Rails• Strong understanding of relational databases (PostgreSQL or MySQL), SQL optimization, and RESTful APIs• Familiarity with testing frameworks such as RSpec, Minitest, or Capybara and background job tools like Sidekiq or Resque• Proficiency with Git and modern development workflows• Experience in debugging and optimizing production systems and delivering intricate features from start to finish• Solid grasp of software architecture, scalability, and clean coding practices• Excellent communication skills to convey technical concepts effectively and collaborate across cross-functional teams• 5+ years of professional software development experience, specifically in Ruby on RailsWhy You’ll Love Working Here• Unlimited paid time off – we trust our employees to maintain work-life balance• Retirement savings support – RRSP/401(k) matching at 100% up to 3%• Comprehensive health benefits including medical, dental, vision, life & disability insurance, and paid parental leave.

Costello Medical is hiring an IT Administrator based in Cambridge, England. This position plays a central role in keeping the company’s IT infrastructure stable and secure, supporting the daily work of teams across the business. Key responsibilities Maintain and oversee IT systems throughout the organization Troubleshoot technical issues, including both hardware and software problems Apply solutions to improve system performance and strengthen security Role focus This role centers on supporting smooth operations by resolving IT challenges and ensuring reliable technology for colleagues. Company mission Costello Medical provides medical communications and data analysis services. The IT Administrator helps support this mission by making sure technology works efficiently and securely.

Join our team at Integrated Resources Inc. as a Technical Writer, where you will play a crucial role in crafting and refining documentation that supports our innovative projects. You will collaborate closely with engineers, product managers, and other stakeholders to ensure that complex technical concepts are conveyed clearly and effectively. Your expertise in writing and editing will help us maintain high standards of quality in our documentation.

Join us at Jobs for Humanity as we seek passionate Speakers and Writers who are ready to inspire and empower diverse communities. Your words can make a difference, driving social change and promoting inclusivity. We value creativity, originality, and the ability to engage audiences effectively.

Amylyx Pharmaceuticals is on a daring mission to transform the landscape of treatments for diseases with significant unmet needs. We embrace challenges as opportunities, driving forward with urgency, rigorous scientific approaches, and a steadfast commitment to the communities we serve. As a clinical-stage organization, we are currently dedicated to addressing post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission is fueled by our exceptional team. We uphold core values of audacity, curiosity, authenticity, engagement, and accountability, fostering a culture of compassion. At Amylyx, we have assembled a skilled team eager to take decisive action, as the communities we serve cannot afford to wait. If you share our passion and are resolute in tackling some of medicine's most challenging problems, we invite you to explore the opportunity below and apply.The OpportunityAmylyx is seeking a Senior Medical Director, Clinical Development to deliver strategic and scientific leadership for one or more late-stage, pivotal programs with the possibility of expanding into additional indications and/or programs within the same molecule or across our portfolio. This role is pivotal in shaping the overall clinical development strategy and may oversee multiple programs or key components of a broader development portfolio.Reporting directly to the Senior VP of Clinical Development, you will be tasked with leading the design, execution, and analysis of clinical studies and managing the development and implementation of Clinical Development Plans across assigned assets. Your strategic input will be crucial in study design, endpoints, and regulatory strategies, ensuring alignment with overall program and corporate objectives.The ideal candidate will work collaboratively with cross-functional teams in a matrix environment, influencing stakeholders across Research, Regulatory Affairs, Clinical Operations, and Commercial to ensure that clinical and scientific considerations are fully integrated into development plans. You will proactively identify and mitigate risks, guide decision-making through data-driven insights, and uphold the highest standards of scientific rigor and data integrity.In this capacity, you will also act as a key external representative, engaging with global medical experts, investigators, regulatory authorities, and alliance partners. You may lead or mentor a team of clinical scientists and physicians and contribute to broader organizational and portfolio-level initiatives.

Your Contribution at Lila Sciences At Lila Sciences, we believe that scientific discoveries only make a meaningful impact when they are effectively communicated. Our Government sector team acts as a vital link between exceptional researchers and the government clients and internal stakeholders who rely on their insights. We are on the lookout for a Physical Science Technical Writer who excels in this pivotal role. In this role, you will report to the Head of Government Partnerships and act as a crucial connector between our scientific team and the stakeholders who support and implement their research findings. You will take complex technical information, methodologies, and data and translate them into clear, credible, and actionable language. Collaborating closely with our Grants Manager, who oversees the proposal process, you will craft the technical and scientific elements that lie at the core of successful submissions. As a quality assurance gatekeeper, you will leverage your domain expertise to identify scientific inaccuracies, challenge vague claims, and ensure that all deliverables adhere to the highest standards of technical excellence before they are finalized. This position transcends mere documentation maintenance; it is a strategic communication role designed for someone with enough scientific acumen to grasp intricate research concepts and the communication prowess to convey them to non-specialist audiences. Importantly, we seek a candidate who is adept at utilizing AI tools as a productivity enhancer: a writer who can harness LLMs, create streamlined automation processes, or design workflow tools that empower individuals to achieve remarkable outcomes. Key Responsibilities Translate Scientific Research for Government StakeholdersEngage directly with Lila's scientists and engineers to fully comprehend their research, then generate briefings, white papers, and executive reports that effectively communicate scientific insights to government clients, program officers, and agency stakeholders, adjusting tone, depth, and format as needed. Proposal and Grant Development SupportCollaborate with the Grants Manager to create the technical and scientific components of proposal applications (technical narratives, methods descriptions, scientific appendices) for initiatives funded by the DOE and UK, ensuring consistency in tone, format, and compliance throughout. Content Repository and Knowledge ManagementDevelop and maintain a repository of reusable, version-controlled technical content, including vetted scientific descriptions, methods summaries, capability statements, and regulatory narratives, to facilitate efficient knowledge transfer.

Join our dynamic team at Integrated Resources Inc. as a skilled Medical Coder. In this pivotal role, you will be responsible for accurately translating healthcare services into standardized codes used for billing and insurance purposes. Your attention to detail and coding expertise will play a crucial role in ensuring proper reimbursement and compliance within the healthcare system.